55030-002 NDC - NATTOGRAPESEEDENZYMEPOWDER

Drug Information

Product NDC: 55030-002

Proprietary Name: NattoGrapeSeedEnzymePowder

Non Proprietary Name: NattoGrapeSeedEnzymePowder

Active Ingredient(s):
  • .25 g/5g ORANGE;
  • .5 g/5g MALTODEXTRIN;
  • .25 g/5g NATTOKINASE;
  • .75 g/5g RED YEAST;
  • .35 g/5g ASCORBIC ACID;
  • 1.25 g/5g STEM BROMELAIN;
  • 1 g/5g ARGININE;
  • .5 g/5g VITIS VINIFERA SEED


Administration Route(s): ORAL

Dosage Form(s): POWDER

Labeler Information

Labeler Name: Shenzhen Aiwei Biological Technology Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/3/2020

Package Information

No. Package Code Package Description Billing Unit
155030-002-0215 PACKAGE in 1 PACKAGE, COMBINATION (55030-002-02) > 5 g in 1 PACKAGE (55030-002-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC55030-002The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMENattoGrapeSeedEnzymePowderThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMENattoGrapeSeedEnzymePowderThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPOWDERThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/3/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEShenzhen Aiwei Biological Technology Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEORANGE; MALTODEXTRIN; NATTOKINASE; RED YEAST; ASCORBIC ACID; STEM BROMELAIN; ARGININE; VITIS VINIFERA SEEDThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.25; .5; .25; .75; .35; 1.25; 1; .5 
ACTIVE INGRED UNITg/5g; g/5g; g/5g; g/5g; g/5g; g/5g; g/5g; g/5g 

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This page was last updated on: 7/26/2021